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HomeCompaniesCareers Rocketpharma Icims ComSpecialist, Quality Document Control

Specialist, Quality Document Control

Careers Rocketpharma Icims Com · Cranbury, NJ, US · On Site · Active · $56,000–$68,000 / year · iCIMS

Job facts

FieldValue
CompanyCareers Rocketpharma Icims Com
TitleSpecialist, Quality Document Control
Normalized title-
Department / teamQuality Assurance
LocationCranbury, NJ, United States
Work modelOn Site
Employment typeFull Time
Salary$56,000–$68,000 / year
Statusactive
ATS provideriCIMS
Posted / first seen2026-04-10 / 2026-05-31
Changed / last seen2026-06-01 / 2026-06-06

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City jobsActive postings in Cranbury.Open
Department jobsActive postings in Quality Assurance.Open
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Linked records

CompanyCareers Rocketpharma Icims Com
Source8f622a14-eebd-483c-84e3-f2ef0672afd5
ATS provideriCIMS

Description

Overview Create a future where DNA is no longer destiny. Join Rocket Pharma. Rocket Pharma is a fully integrated, late-stage biotechnology company advancing gene therapies with curative potential for patients with rare and life-threatening diseases. We are a team of creative, compassionate, and driven individuals united by a profound mission of seeking gene therapy cures. Rocket places tremendous value on our people and fosters a collaborative environment where bold ideas thrive and every team member makes a meaningful impact. Our core values guide everything we do: we trust one another, show generosity toward patients, embrace curiosity, and strive to elevate science. Team members receive a competitive total rewards package, including equity participation, 401(k) matching, and excellent health benefits. Position Summary The Specialist, Quality Document Control will provide support for the management and control of documentation at Rocket including within the ZenQMS electronic quality system. This role will manage all paper-based documents and records and will be the primary owner of the document control storage room that houses all paper records/logbooks, batch records, etc. Responsibilities Management of documents within the ZenQMS electronic quality system. Issuance and archiving of all paper-based documents and records, including batch records, logbooks, controlled forms, etc. Oversight and management of the on-site physical document storage room Support the various functional groups in managing their documents Supporting the ZenQMS team in managing documents within the system Qualifications Associates Degree - Degree in science related field preferred Minimum three years of experience in a document control or document management role Experience with electronic document management systems (ZenQMS, Veeva, etc.) Minimum of 3-5 years of quality biopharma experience Familiar with standard software systems (Microsoft Word, Excel, PowerPoint, etc.) Ability to work within a multifunctional team Work with documents, pushing carts to transport batch records and large sets of documents/binders Compensation The expected salary range for this position is $56,000 to $68,000. At Rocket, our compensation philosophy and ranges are built upon data and insights collected from validated world-class providers. We are committed to compensating employees equitably based on several factors, including responsibilities and level of the position, depth and types of the employee’s experience, location of the position and availability of similar talent in a competitive market. For U.S.-based candidates, this is an at-will position, and Rocket reserves the right to adjust the range at hire or during the year due to market shifts. In addition to base salary, Rocket offers a competitive total rewards package that may include bonuses (short-term incentives), medical, dental, and vision insurance, life insurance, 401(k) with company match and generous vesting, paid vacation and holidays, global shutdown days between Christmas and New Year’s, and a variety of wellness resources and employee support programs. Also, certain positions are eligible for added forms of compensation, such equity awards (long-term incentives). EEO Statement A diverse workforce fosters innovation and strengthens Rocket’s business. We ensure equal opportunity without discrimination or harassment in the workplace on the basis of gender, race, color, religion, national origin, age, physical or mental disability, pregnancy, citizenship, status as a protected veteran, marital status, sexual orientation, gender identity and expression, genetic information, or any other characteristic protected by applicable local, state, and federal laws.

Full job record

Job ID1d5cf11da33c2fbc290ce3d809281977ce9f56cd
Org ID9d2b7a1a-62cd-42b3-906a-0d84c2de80e1
Source ID8f622a14-eebd-483c-84e3-f2ef0672afd5
Board ID8f622a14-eebd-483c-84e3-f2ef0672afd5
Providericims
Provider Job Key2129
TitleSpecialist, Quality Document Control
Normalized Title
Statusactive
Activeyes
Location TextCranbury, NJ, US
DepartmentQuality Assurance
Team
Employment Typefull_time
Workplace Typeon_site
Remote Policy
CountryUnited States
RegionNJ
CityCranbury
Salary RawOverview Create a future where DNA is no longer destiny. Join Rocket Pharma. Rocket Pharma is a fully integrated, late-stage biotechnology company advancing gene therapies with curative potential for patients with rare and life-threatening diseases. We are a team of creative, compassionate, and driven individuals united by a profound mission of seeking gene therapy cures. Rocket places tremendous value on our people and fosters a collaborative environment where bold ideas thrive and every team member makes a meaningful impact. Our core values guide everything we do: we trust one another, show generosity toward patients, embrace curiosity, and strive to elevate science. Team members receive a competitive total rewards package, including equity participation, 401(k) matching, and excellent health benefits. Position Summary The Specialist, Quality Document Control will provide support for the management and control of documentation at Rocket including within the ZenQMS electronic quality system. This role will manage all paper-based documents and records and will be the primary owner of the document control storage room that houses all paper records/logbooks, batch records, etc. Responsibilities Management of documents within the ZenQMS electronic quality system. Issuance and archiving of all paper-based documents and records, including batch records, logbooks, controlled forms, etc. Oversight and management of the on-site physical document storage room Support the various functional groups in managing their documents Supporting the ZenQMS team in managing documents within the system Qualifications Associates Degree - Degree in science related field preferred Minimum three years of experience in a document control or document management role Experience with electronic document management systems (ZenQMS, Veeva, etc.) Minimum of 3-5 years of quality biopharma experience Familiar with standard software systems (Microsoft Word, Excel, PowerPoint, etc.) Ability to work within a multifunctional team Work with documents, pushing carts to transport batch records and large sets of documents/binders Compensation The expected salary range for this position is $56,000 to $68,000. At Rocket, our compensation philosophy and ranges are built upon data and insights collected from validated world-class providers. We are committed to compensating employees equitably based on several factors, including responsibilities and level of the position, depth and types of the employee’s experience, location of the position and availability of similar talent in a competitive market. For U.S.-based candidates, this is an at-will position, and Rocket reserves the right to adjust the range at hire or during the year due to market shifts. In addition to base salary, Rocket offers a competitive total rewards package that may include bonuses (short-term incentives), medical, dental, and vision insurance, life insurance, 401(k) with company match and generous vesting, paid vacation and holidays, global shutdown days between Christmas and New Year’s, and a variety of wellness resources and employee support programs. Also, certain positions are eligible for added forms of compensation, such equity awards (long-term incentives). EEO Statement A diverse workforce fosters innovation and strengthens Rocket’s business. We ensure equal opportunity without discrimination or harassment in the workplace on the basis of gender, race, color, religion, national origin, age, physical or mental disability, pregnancy, citizenship, status as a protected veteran, marital status, sexual orientation, gender identity and expression, genetic information, or any other characteristic protected by applicable local, state, and federal laws.
Salary Min56,000
Salary Max68,000
Salary CurrencyUSD
Salary Periodyear
Source URLhttps://careers-rocketpharma.icims.com/jobs/2129/specialist%2c-quality-document-control/job
Apply URLhttps://careers-rocketpharma.icims.com/jobs/2129/specialist%2c-quality-document-control/job
First Seen At2026-05-31 18:43:28Z
Last Seen At2026-06-06 08:29:08Z
Last Checked At2026-06-06 08:29:08Z
Last Changed At2026-06-01 13:59:05Z
Inactive At
Source Posted At2026-04-10 04:00:00Z
Source Updated At2026-04-14 14:07:46Z
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Parsed Structured
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Extensions
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